Centurion Medical recalls Cap Change Kit DT20310 due to potential fluid droplets separating after disconnection. Affected units sold in 2017. No remedy specified in official notice.
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Centurion Medical is recalling their Cap Change Kit DT20310 because it may cause fluid droplets to separate from the connector after disconnection. This could lead to contamination risks during medical procedures. The recall affects specific model numbers sold in 2017.
The BD MaxZeroNeedleless Connector in the kit may release fluid droplets when disconnected. This could cause contamination during medical procedures if the droplets come into contact with the patient or environment.
Healthcare professionals using the Cap Change Kit DT20310 for medical procedures are most at risk. Patients receiving care with this kit could be exposed to potential contamination.
Check for model numbers 2017032780, 2017052280, 2017070380, 2017072480, or 2017091180 on the kit. These units were sold starting in 2017.
Look for specific model numbers listed in the recall notice: 2017032780, 2017052280, 2017070380, 2017072480, or 2017091180.
The official recall notice does not specify any remedy.
The affected model numbers are 2017032780, 2017052280, 2017070380, 2017072480, and 2017091180.
These units were sold starting in 2017.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0081-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0081-2020 from Centurion Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
